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Large Visual Stimuli Induce Two Distinct Gamma Oscillations in Primate Visual Cortex

Recent studies have shown the existence of two gamma rhythms in the hippocampus subserving different functions but, to date, primate studies in primary visual cortex have reported a single gamma rhythm. Here, we show that large visual stimuli induce a slow gamma (25–45 Hz) in area V1 of two awake ad...

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Autores principales: Murty, Dinavahi V.P.S., Shirhatti, Vinay, Ravishankar, Poojya, Ray, Supratim
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Society for Neuroscience 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5852657/
https://www.ncbi.nlm.nih.gov/pubmed/29440388
http://dx.doi.org/10.1523/JNEUROSCI.2270-17.2017
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author Murty, Dinavahi V.P.S.
Shirhatti, Vinay
Ravishankar, Poojya
Ray, Supratim
author_facet Murty, Dinavahi V.P.S.
Shirhatti, Vinay
Ravishankar, Poojya
Ray, Supratim
author_sort Murty, Dinavahi V.P.S.
collection PubMed
description Recent studies have shown the existence of two gamma rhythms in the hippocampus subserving different functions but, to date, primate studies in primary visual cortex have reported a single gamma rhythm. Here, we show that large visual stimuli induce a slow gamma (25–45 Hz) in area V1 of two awake adult female bonnet monkeys and in the EEG of 15 human subjects (7 males and 8 females), in addition to the traditionally known fast gamma (45–70 Hz). The two rhythms had different tuning characteristics for stimulus orientation, contrast, drift speed, and size. Further, fast gamma had short latency, strongly entrained spikes and was coherent over short distances, reflecting short-range processing, whereas slow gamma appeared to reflect long-range processing. Together, two gamma rhythms can potentially provide better coding or communication mechanisms and a more comprehensive biomarker for diagnosis of mental disorders. SIGNIFICANCE STATEMENT Gamma rhythm has been associated with high-level cognitive functions such as attention and feature binding and has been reported to be abnormal in brain disorders such as autism and schizophrenia. Unlike previous studies that have shown a single gamma rhythm in the primate visual cortex, we found that large visual gratings induce two distinct gamma oscillations in both monkey LFP and human EEG. These rhythms, termed slow (25–45 Hz) and fast (45–70 Hz), exhibited distinct tuning preferences, latencies, and coherence profiles, potentially reflecting processing at two different ranges. Multiple gamma oscillations in visual cortex may provide a richer representation of external visual stimuli and could be used for developing brain–machine interfacing applications and screening tests for neuropsychiatric disorders.
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spelling pubmed-58526572018-03-22 Large Visual Stimuli Induce Two Distinct Gamma Oscillations in Primate Visual Cortex Murty, Dinavahi V.P.S. Shirhatti, Vinay Ravishankar, Poojya Ray, Supratim J Neurosci Research Articles Recent studies have shown the existence of two gamma rhythms in the hippocampus subserving different functions but, to date, primate studies in primary visual cortex have reported a single gamma rhythm. Here, we show that large visual stimuli induce a slow gamma (25–45 Hz) in area V1 of two awake adult female bonnet monkeys and in the EEG of 15 human subjects (7 males and 8 females), in addition to the traditionally known fast gamma (45–70 Hz). The two rhythms had different tuning characteristics for stimulus orientation, contrast, drift speed, and size. Further, fast gamma had short latency, strongly entrained spikes and was coherent over short distances, reflecting short-range processing, whereas slow gamma appeared to reflect long-range processing. Together, two gamma rhythms can potentially provide better coding or communication mechanisms and a more comprehensive biomarker for diagnosis of mental disorders. SIGNIFICANCE STATEMENT Gamma rhythm has been associated with high-level cognitive functions such as attention and feature binding and has been reported to be abnormal in brain disorders such as autism and schizophrenia. Unlike previous studies that have shown a single gamma rhythm in the primate visual cortex, we found that large visual gratings induce two distinct gamma oscillations in both monkey LFP and human EEG. These rhythms, termed slow (25–45 Hz) and fast (45–70 Hz), exhibited distinct tuning preferences, latencies, and coherence profiles, potentially reflecting processing at two different ranges. Multiple gamma oscillations in visual cortex may provide a richer representation of external visual stimuli and could be used for developing brain–machine interfacing applications and screening tests for neuropsychiatric disorders. Society for Neuroscience 2018-03-14 /pmc/articles/PMC5852657/ /pubmed/29440388 http://dx.doi.org/10.1523/JNEUROSCI.2270-17.2017 Text en Copyright © 2018 Murty et al. https://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License Creative Commons Attribution 4.0 International (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution and reproduction in any medium provided that the original work is properly attributed.
spellingShingle Research Articles
Murty, Dinavahi V.P.S.
Shirhatti, Vinay
Ravishankar, Poojya
Ray, Supratim
Large Visual Stimuli Induce Two Distinct Gamma Oscillations in Primate Visual Cortex
title Large Visual Stimuli Induce Two Distinct Gamma Oscillations in Primate Visual Cortex
title_full Large Visual Stimuli Induce Two Distinct Gamma Oscillations in Primate Visual Cortex
title_fullStr Large Visual Stimuli Induce Two Distinct Gamma Oscillations in Primate Visual Cortex
title_full_unstemmed Large Visual Stimuli Induce Two Distinct Gamma Oscillations in Primate Visual Cortex
title_short Large Visual Stimuli Induce Two Distinct Gamma Oscillations in Primate Visual Cortex
title_sort large visual stimuli induce two distinct gamma oscillations in primate visual cortex
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5852657/
https://www.ncbi.nlm.nih.gov/pubmed/29440388
http://dx.doi.org/10.1523/JNEUROSCI.2270-17.2017
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